Evidence map›Paper›PMID 24231259›Full record

ArticleJournal of leukocyte biology2014

Virus-specific CD4 and CD8 T cell responses in the absence of Th1-associated transcription factors.

Sarah B Mollo, Jennifer T Ingram, Robert L Kress, Allan J Zajac, Laurie E Harrington

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Memory T-Cell Heterogeneity and Terminology.Cold Spring Harbor perspectives in biology · 2021
    Review
  6. Article
  7. Delineation of a molecularly distinct terminally differentiated memory CD8 T cell population.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Article
  9. Memory CD4Cells · 2020
    Review
  10. MicroRNA regulation of CD8Non-coding RNA investigation · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sarah B MolloDepartments of Cell, Developmental, and Integrative Biology.
Jennifer T IngramBiology, and.
Robert L KressDepartments of Cell, Developmental, and Integrative Biology.
Allan J ZajacMicrobiology, University of Alabama at Birmingham, Alabama, USA.
Laurie E HarringtonDepartments of Cell, Developmental, and Integrative Biology, lharring@uab.edu.
University of Alabama at Birmingham · US

Funding

IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
IL- 21 and Immune Mediated Viral ControlU01AI082966 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ZAJAC, ALLAN J · 2009 to 2013
$2.3M
Regulation of effector CD4 T cell subsets during inflammatory bowel diseaseR01DK084082 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARRINGTON, LAURIE ELLEN · 2010 to 2014
$1.6M
NIAID NIH HHS T32 AI007051NIAID NIH HHS U01 AI082966NIAMS NIH HHS P30 AR048311NIDDK NIH HHS R01 DK084082
6 · The paper itself

Abstract

Effector and memory CD4 and CD8 T cell responses are critical for the control of many intracellular pathogens. The development of these populations is governed by transcription factors that molecularly control their differentiation, function, and maintenance. Two transcription factors known to be involved in these processes are Tbet and STAT4. Although Tbet has been shown to regulate CD8 T cell fate decisions and effector CD4 T cell choices, the contribution of STAT4 is less well understood. To address this, we examined the impact of STAT4 on T cell responses in the presence or absence of Tbet, following LCMV infection by using mice lacking Tbet, STAT4, or both transcription factors. STAT4 was not required for Tbet or Eomes expression; however, virus-specific effector CD8 T cells are skewed toward a memory-precursor phenotype in the absence of STAT4. This altered proportion of memory precursors did not result in an increase in memory CD8 T cells after the resolution of the infection. We also demonstrate that virus-specific effector and memory CD4 T cells formed independently of Tbet and STAT4, although a slight reduction in the number of antigen-specific CD4 T cells was apparent in mice lacking both transcription factors. Collectively, we have discovered distinct roles for Tbet and STAT4 in shaping the phenotype and function of virus-specific T cell responses.

Indexed as

AnimalsCD8-Positive T-LymphocytesLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, Inbred BALB CMice, KnockoutSTAT4 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinsTh1 CellsStat4 protein, mouseSTAT4 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinscytokineseffectorLCMVmemorySTAT4Tbet

Identifiers

PMID24231259
PMCPMC3984968
OpenAlexW2138238271

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.